9p24.3-p13.3CNV Type: Duplication
Largest CNV size: 33677109 bp
Statistics Box:
Number of Reports: 3
Number of Reports: 3
Summary Information
Summary statement in development
Additional Locus Information
References
Major Reports
Title
Author, Year
Report Class
CNV Type
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Duplication
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Duplication
Minor Reports
Title
Author, Year
Report Class
CNV Type
Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability.
Duplication
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
kaminsky_11_DD/ID/ASD_discovery_cases
Cases from the International Standards for Cytogenomic Arrays (ISCA) consortium
15749
Unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome
NA
NA
34395242
0
2
2
sansovic_17_DD/ID/ASD_discovery_cases
Unrelated patients from Croatia referred to the Department of Medical Genetics and Reproductive Health, Children's Hospital Zagreb, University of Zagreb School of Medicine
337
Cases diagnosed by clinical geneticists or pediatricians to have developmental delay/intellectual disability (DD/ID), ASD, congenital anomalies, or a combination of those features
Mean, 7 years (range, 1 month-25 years)
N/A
34002000
0
1
1
szatmari_07_ASD_discovery_cases
ASD patients from 173 families with at least two affected individuals from AGP
196
Patients diagnosed with ASD based on ADI-R and ADOS
33677109
0
1
1
Controls
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
kaminsky_11_DD/ID/ASD_discovery_controls
Controls from the International Standards for Cytogenomic Arrays (ISCA) consortium
10118
Controls
NA
NA
NA
NA
NA
NA
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
kaminsky_11_DD/ID/ASD_discovery_cases
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
FISH, qPCR, MLPA, aCGH, standard G-banded chromosome analysis
sansovic_17_DD/ID/ASD_discovery_cases
Croatia
aCGH
Agilent SurePrint G3 Unrestricted CGH ISCA v2
Agilent Feature Extraction (v12.0), Agilent CytoGenomics (v3.0 and v4.0)
None
szatmari_07_ASD_discovery_cases
Array SNP
Affymetrix 10K (v2)
HMM
dChip
Karyotyping, qPCR, aCGH, array SNP, overlap with Mendelian genotype errors
Controls
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
kaminsky_11_DD/ID/ASD_discovery_controls
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
Cases
Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004306
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
204193
34599437
34395245
GRCh38
Duplication
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004621
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
204193
33284638
33080446
GRCh38
Duplication
Yes
sansovic_17_DD/ID/ASD_discovery_cases-case10
1 yr.
M
Developmental delay/intellectual disability
Developmental delay/intellectual disability, Congenital anomalies, Dysmorphism
204193
34206655
34002463
GRCh38
Duplication
No
szatmari_07_ASD_discovery_cases-NAAR064-F6-HI2067
NA
ASD
NA
NA
249391
33926502
33677112
GRCh38
Duplication
Yes
Controls
No Control Data Available
Cases
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004306
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
RPL12P25,RNU6-1327P,EIF1P1,RNU6-1073P,DMRT2,RPS27AP14,RNA5SP279,RNU2-25P,RN7SL592P,GPS2P1,ATP5PDP2,RNU6-694P,PLPP6,CDC37L1-DT,ECM1P1,KLF4P1,MIR101-2,HNRNPA1P41,CSNK1G2P1,PDSS1P1,MTND6P5,MTND1P11,MTCO1P11,MTCO2P11,MTATP6P11,MTCO3P11,MTND4P14,MTND5P14,IGHEP2,INSL4,RLN2,HMGN2P31,RLN1,RNF152P1,AK4P4,MIR4665,GTF3AP1,SELENOTP1,TPD52L3,RN7SL25P,RPL23AP57,RN7SL123P,RPS3AP54,RNF2P1,PRELID3BP11,SNRPEP2,ACTG1P14,RPL4P5,PPIAP33,RNU7-185P,PTPRD-AS1,RPS26P3,RN7SL5P,AKAP8P1,RNU2-47P,RN7SL849P,PRDX1P1,PES1P2,ATP5PDP3,CDCA4P1,CER1,RNU6-1260P,LDHAP4,RNU6-559P,RPL7P33,RNU6-319P,RN7SL98P,FTH1P12,RNU6-246P,HMGN2P16,RNU6-14P,BNC2-AS1,LSM1P1,RN7SL720P,RPS29P33,SAMM50P1,PABPC1P11,MIR3152,RN7SKP258,RAP1BP1,RRAGA,SCARNA8,RNU6-264P,RPS6,NDUFA5P3,C11orf98P1,MIR4473,RNU4-26P,MIR4474,FOCAD-AS1,MIR491,SNORA30B,IFNNP1,IFNB1,IFNWP4,IFNW1,IFNA21,IFNWP15,IFNA4,IFNWP9,IFNA7,IFNA10,IFNWP18,IFNA17,IFNWP5,IFNA14,IFNA22P,IFNA5,IFNA20P,IFNA6,IFNA13,IFNA2,IFNA11P,IFNA12P,IFNA8,IFNWP2,IFNA1,IFNWP19,IFNE,MIR31,KHSRPP1,RN7SL151P,TUBB8P1,ERVFRD-3,CDKN2A-DT,UBA52P6,DMRTA1,CLIC4P1,SUMO2P2,NOP56P2,RMRPP5,RN7SKP120,TUSC1,FAM71BP1,RN7SL100P,IFT74-AS1,RNA5SP280,CTAGE12P,KCTD10P1,MIR876,MIR873,ME2P1,SLC4A1APP1,C2orf27AP2,RBMXP2,KRT18P66,KRT18P36,RPS26P2,FTLP4,HSPA8P17,SLC25A6P2,MTATP6P30,HMGB3P23,RNA5SP281,SLC25A5P8,TOPORS,DFFBP1,TAF1L,SNRPCP1,BOLA3P4,ASS1P12,TCEA1P4,LAGE3P1,RNU4ATAC15P,AQP3,MIR6851,SNX18P7,PRSS3P4,TRBV20OR9-2,ANXA2P2,TRBV21OR9-2,TRBV22OR9-2,TRBV23OR9-2,TRBV24OR9-2,TRBV25OR9-2,PTENP1,TRBV26OR9-2,TRBV29OR9-2,RNU4ATAC11P,SNORD121B,SNORD121A,OSTCP8,RN7SKP114,TUBB4BP2,RNA5SP282,RNU2-50P,SERPINH1P1,RN7SKP24,C9orf66,DMRT3,VLDLR,KCNV2,LINC01231,GLIS3-AS1,SLC1A1,CDC37L1,INSL6,CD274,PDCD1LG2,RANBP6,IL33,IMP3P1,JKAMPP1,TYRP1,LURAP1L,LINC01235,LINC00583,RPL3P11,SNAPC3,HAUS6,ACER2,MAP1LC3BP1,HACD4,IFNA16,KLHL9,CDKN2A,CDKN2B,IZUMO3,LINC01241,PLAA,EQTN,C9orf72,LINC01243,MTCO3P30,ACO1,SMIM27,NDUFB6,TMEM215,APTX,SMU1,B4GALT1-AS1,SPINK4,BAG1,CHMP5,AQP7,NOL6,SUGT1P1,CYP4F26P,LINC01251,PRSS3,UBE2R2,DCAF12,KIF24,MYORG,C9orf24,FAM219A,ENHO,CNTFR,CNTFR-AS1,DOCK8,KANK1,DMRT1,VLDLR-AS1,PUM3,CARM1P1,RFX3,RFX3-AS1,SPATA6L,AK3,RCL1,JAK2,TCF3P1,PLGRKT,RIC1,ERMP1,KIAA2026,MLANA,UHRF2,GLDC,KDM4C,DMAC1,PTPRD-AS2,LURAP1L-AS1,MPDZ,NFIB,FREM1,CLCN3P1,TTC39B,PSIP1,C9orf92,CNTLN,SH3GL2,PLIN2,DENND4C,SLC24A2,MLLT3,MIR31HG,MTAP,LINC01239,ELAVL2,CAAP1,IFT74,LRRC19,TEK,MOB3B,IFNK,DNAJA1,B4GALT1,NFX1,PTENP1-AS,UBE2R2-AS1,UBAP2,UBAP1,NUDT2,DNAI1,LINC01230,SMARCA2,GLIS3,ZDHHC21,CCDC171,ADAMTSL1,SAXO1,FOCAD,CDKN2B-AS1,LINC00032,LINGO2,LINC01242,DDX58,PTPRD,BNC2,ANKRD18B
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004621
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Paternal
Unknown
Unknown
RPL12P25,RNU6-1327P,EIF1P1,RNU6-1073P,DMRT2,RPS27AP14,RNA5SP279,RNU2-25P,RN7SL592P,GPS2P1,ATP5PDP2,RNU6-694P,PLPP6,CDC37L1-DT,ECM1P1,KLF4P1,MIR101-2,HNRNPA1P41,CSNK1G2P1,PDSS1P1,MTND6P5,MTND1P11,MTCO1P11,MTCO2P11,MTATP6P11,MTCO3P11,MTND4P14,MTND5P14,IGHEP2,INSL4,RLN2,HMGN2P31,RLN1,RNF152P1,AK4P4,MIR4665,GTF3AP1,SELENOTP1,TPD52L3,RN7SL25P,RPL23AP57,RN7SL123P,RPS3AP54,RNF2P1,PRELID3BP11,SNRPEP2,ACTG1P14,RPL4P5,PPIAP33,RNU7-185P,PTPRD-AS1,RPS26P3,RN7SL5P,AKAP8P1,RNU2-47P,RN7SL849P,PRDX1P1,PES1P2,ATP5PDP3,CDCA4P1,CER1,RNU6-1260P,LDHAP4,RNU6-559P,RPL7P33,RNU6-319P,RN7SL98P,FTH1P12,RNU6-246P,HMGN2P16,RNU6-14P,BNC2-AS1,LSM1P1,RN7SL720P,RPS29P33,SAMM50P1,PABPC1P11,MIR3152,RN7SKP258,RAP1BP1,RRAGA,SCARNA8,RNU6-264P,RPS6,NDUFA5P3,C11orf98P1,MIR4473,RNU4-26P,MIR4474,FOCAD-AS1,MIR491,SNORA30B,IFNNP1,IFNB1,IFNWP4,IFNW1,IFNA21,IFNWP15,IFNA4,IFNWP9,IFNA7,IFNA10,IFNWP18,IFNA17,IFNWP5,IFNA14,IFNA22P,IFNA5,IFNA20P,IFNA6,IFNA13,IFNA2,IFNA11P,IFNA12P,IFNA8,IFNWP2,IFNA1,IFNWP19,IFNE,MIR31,KHSRPP1,RN7SL151P,TUBB8P1,ERVFRD-3,CDKN2A-DT,UBA52P6,DMRTA1,CLIC4P1,SUMO2P2,NOP56P2,RMRPP5,RN7SKP120,TUSC1,FAM71BP1,RN7SL100P,IFT74-AS1,RNA5SP280,CTAGE12P,KCTD10P1,MIR876,MIR873,ME2P1,SLC4A1APP1,C2orf27AP2,RBMXP2,KRT18P66,KRT18P36,RPS26P2,FTLP4,HSPA8P17,SLC25A6P2,MTATP6P30,HMGB3P23,RNA5SP281,SLC25A5P8,TOPORS,DFFBP1,TAF1L,SNRPCP1,BOLA3P4,ASS1P12,TCEA1P4,LAGE3P1,RNU4ATAC15P,C9orf66,DMRT3,VLDLR,KCNV2,LINC01231,GLIS3-AS1,SLC1A1,CDC37L1,INSL6,CD274,PDCD1LG2,RANBP6,IL33,IMP3P1,JKAMPP1,TYRP1,LURAP1L,LINC01235,LINC00583,RPL3P11,SNAPC3,HAUS6,ACER2,MAP1LC3BP1,HACD4,IFNA16,KLHL9,CDKN2A,CDKN2B,IZUMO3,LINC01241,PLAA,EQTN,C9orf72,LINC01243,MTCO3P30,ACO1,SMIM27,NDUFB6,TMEM215,APTX,SMU1,B4GALT1-AS1,SPINK4,BAG1,CHMP5,DOCK8,KANK1,DMRT1,VLDLR-AS1,PUM3,CARM1P1,RFX3,RFX3-AS1,SPATA6L,AK3,RCL1,JAK2,TCF3P1,PLGRKT,RIC1,ERMP1,KIAA2026,MLANA,UHRF2,GLDC,KDM4C,DMAC1,PTPRD-AS2,LURAP1L-AS1,MPDZ,NFIB,FREM1,CLCN3P1,TTC39B,PSIP1,C9orf92,CNTLN,SH3GL2,PLIN2,DENND4C,SLC24A2,MLLT3,MIR31HG,MTAP,LINC01239,ELAVL2,CAAP1,IFT74,LRRC19,TEK,MOB3B,IFNK,DNAJA1,B4GALT1,LINC01230,SMARCA2,GLIS3,ZDHHC21,CCDC171,ADAMTSL1,SAXO1,FOCAD,CDKN2B-AS1,LINC00032,LINGO2,LINC01242,DDX58,PTPRD,BNC2
sansovic_17_DD/ID/ASD_discovery_cases-case10
De novo
RPL12P25,RNU6-1327P,EIF1P1,RNU6-1073P,DMRT2,RPS27AP14,RNA5SP279,RNU2-25P,RN7SL592P,GPS2P1,ATP5PDP2,RNU6-694P,PLPP6,CDC37L1-DT,ECM1P1,KLF4P1,MIR101-2,HNRNPA1P41,CSNK1G2P1,PDSS1P1,MTND6P5,MTND1P11,MTCO1P11,MTCO2P11,MTATP6P11,MTCO3P11,MTND4P14,MTND5P14,IGHEP2,INSL4,RLN2,HMGN2P31,RLN1,RNF152P1,AK4P4,MIR4665,GTF3AP1,SELENOTP1,TPD52L3,RN7SL25P,RPL23AP57,RN7SL123P,RPS3AP54,RNF2P1,PRELID3BP11,SNRPEP2,ACTG1P14,RPL4P5,PPIAP33,RNU7-185P,PTPRD-AS1,RPS26P3,RN7SL5P,AKAP8P1,RNU2-47P,RN7SL849P,PRDX1P1,PES1P2,ATP5PDP3,CDCA4P1,CER1,RNU6-1260P,LDHAP4,RNU6-559P,RPL7P33,RNU6-319P,RN7SL98P,FTH1P12,RNU6-246P,HMGN2P16,RNU6-14P,BNC2-AS1,LSM1P1,RN7SL720P,RPS29P33,SAMM50P1,PABPC1P11,MIR3152,RN7SKP258,RAP1BP1,RRAGA,SCARNA8,RNU6-264P,RPS6,NDUFA5P3,C11orf98P1,MIR4473,RNU4-26P,MIR4474,FOCAD-AS1,MIR491,SNORA30B,IFNNP1,IFNB1,IFNWP4,IFNW1,IFNA21,IFNWP15,IFNA4,IFNWP9,IFNA7,IFNA10,IFNWP18,IFNA17,IFNWP5,IFNA14,IFNA22P,IFNA5,IFNA20P,IFNA6,IFNA13,IFNA2,IFNA11P,IFNA12P,IFNA8,IFNWP2,IFNA1,IFNWP19,IFNE,MIR31,KHSRPP1,RN7SL151P,TUBB8P1,ERVFRD-3,CDKN2A-DT,UBA52P6,DMRTA1,CLIC4P1,SUMO2P2,NOP56P2,RMRPP5,RN7SKP120,TUSC1,FAM71BP1,RN7SL100P,IFT74-AS1,RNA5SP280,CTAGE12P,KCTD10P1,MIR876,MIR873,ME2P1,SLC4A1APP1,C2orf27AP2,RBMXP2,KRT18P66,KRT18P36,RPS26P2,FTLP4,HSPA8P17,SLC25A6P2,MTATP6P30,HMGB3P23,RNA5SP281,SLC25A5P8,TOPORS,DFFBP1,TAF1L,SNRPCP1,BOLA3P4,ASS1P12,TCEA1P4,LAGE3P1,RNU4ATAC15P,AQP3,MIR6851,SNX18P7,PRSS3P4,TRBV20OR9-2,ANXA2P2,TRBV21OR9-2,TRBV22OR9-2,TRBV23OR9-2,TRBV24OR9-2,TRBV25OR9-2,PTENP1,TRBV26OR9-2,TRBV29OR9-2,RNU4ATAC11P,SNORD121B,SNORD121A,OSTCP8,RN7SKP114,TUBB4BP2,RNA5SP282,C9orf66,DMRT3,VLDLR,KCNV2,LINC01231,GLIS3-AS1,SLC1A1,CDC37L1,INSL6,CD274,PDCD1LG2,RANBP6,IL33,IMP3P1,JKAMPP1,TYRP1,LURAP1L,LINC01235,LINC00583,RPL3P11,SNAPC3,HAUS6,ACER2,MAP1LC3BP1,HACD4,IFNA16,KLHL9,CDKN2A,CDKN2B,IZUMO3,LINC01241,PLAA,EQTN,C9orf72,LINC01243,MTCO3P30,ACO1,SMIM27,NDUFB6,TMEM215,APTX,SMU1,B4GALT1-AS1,SPINK4,BAG1,CHMP5,AQP7,NOL6,SUGT1P1,CYP4F26P,LINC01251,PRSS3,UBE2R2,DCAF12,DOCK8,KANK1,DMRT1,VLDLR-AS1,PUM3,CARM1P1,RFX3,RFX3-AS1,SPATA6L,AK3,RCL1,JAK2,TCF3P1,PLGRKT,RIC1,ERMP1,KIAA2026,MLANA,UHRF2,GLDC,KDM4C,DMAC1,PTPRD-AS2,LURAP1L-AS1,MPDZ,NFIB,FREM1,CLCN3P1,TTC39B,PSIP1,C9orf92,CNTLN,SH3GL2,PLIN2,DENND4C,SLC24A2,MLLT3,MIR31HG,MTAP,LINC01239,ELAVL2,CAAP1,IFT74,LRRC19,TEK,MOB3B,IFNK,DNAJA1,B4GALT1,NFX1,PTENP1-AS,UBE2R2-AS1,UBAP2,UBAP1,LINC01230,SMARCA2,GLIS3,ZDHHC21,CCDC171,ADAMTSL1,SAXO1,FOCAD,CDKN2B-AS1,LINC00032,LINGO2,LINC01242,DDX58,PTPRD,BNC2,ANKRD18B
szatmari_07_ASD_discovery_cases-NAAR064-F6-HI2067
Karyotyping, qPCR, aCGH, array SNP, or overlap with Mendelian genotype errors
Unknown
NA
NA
RPL12P25,RNU6-1327P,EIF1P1,RNU6-1073P,DMRT2,RPS27AP14,RNA5SP279,RNU2-25P,RN7SL592P,GPS2P1,ATP5PDP2,RNU6-694P,PLPP6,CDC37L1-DT,ECM1P1,KLF4P1,MIR101-2,HNRNPA1P41,CSNK1G2P1,PDSS1P1,MTND6P5,MTND1P11,MTCO1P11,MTCO2P11,MTATP6P11,MTCO3P11,MTND4P14,MTND5P14,IGHEP2,INSL4,RLN2,HMGN2P31,RLN1,RNF152P1,AK4P4,MIR4665,GTF3AP1,SELENOTP1,TPD52L3,RN7SL25P,RPL23AP57,RN7SL123P,RPS3AP54,RNF2P1,PRELID3BP11,SNRPEP2,ACTG1P14,RPL4P5,PPIAP33,RNU7-185P,PTPRD-AS1,RPS26P3,RN7SL5P,AKAP8P1,RNU2-47P,RN7SL849P,PRDX1P1,PES1P2,ATP5PDP3,CDCA4P1,CER1,RNU6-1260P,LDHAP4,RNU6-559P,RPL7P33,RNU6-319P,RN7SL98P,FTH1P12,RNU6-246P,HMGN2P16,RNU6-14P,BNC2-AS1,LSM1P1,RN7SL720P,RPS29P33,SAMM50P1,PABPC1P11,MIR3152,RN7SKP258,RAP1BP1,RRAGA,SCARNA8,RNU6-264P,RPS6,NDUFA5P3,C11orf98P1,MIR4473,RNU4-26P,MIR4474,FOCAD-AS1,MIR491,SNORA30B,IFNNP1,IFNB1,IFNWP4,IFNW1,IFNA21,IFNWP15,IFNA4,IFNWP9,IFNA7,IFNA10,IFNWP18,IFNA17,IFNWP5,IFNA14,IFNA22P,IFNA5,IFNA20P,IFNA6,IFNA13,IFNA2,IFNA11P,IFNA12P,IFNA8,IFNWP2,IFNA1,IFNWP19,IFNE,MIR31,KHSRPP1,RN7SL151P,TUBB8P1,ERVFRD-3,CDKN2A-DT,UBA52P6,DMRTA1,CLIC4P1,SUMO2P2,NOP56P2,RMRPP5,RN7SKP120,TUSC1,FAM71BP1,RN7SL100P,IFT74-AS1,RNA5SP280,CTAGE12P,KCTD10P1,MIR876,MIR873,ME2P1,SLC4A1APP1,C2orf27AP2,RBMXP2,KRT18P66,KRT18P36,RPS26P2,FTLP4,HSPA8P17,SLC25A6P2,MTATP6P30,HMGB3P23,RNA5SP281,SLC25A5P8,TOPORS,DFFBP1,TAF1L,SNRPCP1,BOLA3P4,ASS1P12,TCEA1P4,LAGE3P1,RNU4ATAC15P,AQP3,MIR6851,SNX18P7,PRSS3P4,TRBV20OR9-2,ANXA2P2,TRBV21OR9-2,TRBV22OR9-2,TRBV23OR9-2,TRBV24OR9-2,TRBV25OR9-2,PTENP1,TRBV26OR9-2,TRBV29OR9-2,RNU4ATAC11P,DMRT3,VLDLR,KCNV2,LINC01231,GLIS3-AS1,SLC1A1,CDC37L1,INSL6,CD274,PDCD1LG2,RANBP6,IL33,IMP3P1,JKAMPP1,TYRP1,LURAP1L,LINC01235,LINC00583,RPL3P11,SNAPC3,HAUS6,ACER2,MAP1LC3BP1,HACD4,IFNA16,KLHL9,CDKN2A,CDKN2B,IZUMO3,LINC01241,PLAA,EQTN,C9orf72,LINC01243,MTCO3P30,ACO1,SMIM27,NDUFB6,TMEM215,APTX,SMU1,B4GALT1-AS1,SPINK4,BAG1,CHMP5,AQP7,NOL6,SUGT1P1,CYP4F26P,LINC01251,PRSS3,UBE2R2,DOCK8,KANK1,DMRT1,VLDLR-AS1,PUM3,CARM1P1,RFX3,RFX3-AS1,SPATA6L,AK3,RCL1,JAK2,TCF3P1,PLGRKT,RIC1,ERMP1,KIAA2026,MLANA,UHRF2,GLDC,KDM4C,DMAC1,PTPRD-AS2,LURAP1L-AS1,MPDZ,NFIB,FREM1,CLCN3P1,TTC39B,PSIP1,C9orf92,CNTLN,SH3GL2,PLIN2,DENND4C,SLC24A2,MLLT3,MIR31HG,MTAP,LINC01239,ELAVL2,CAAP1,IFT74,LRRC19,TEK,MOB3B,IFNK,DNAJA1,B4GALT1,NFX1,PTENP1-AS,UBE2R2-AS1,UBAP2,LINC01230,SMARCA2,GLIS3,ZDHHC21,CCDC171,ADAMTSL1,SAXO1,FOCAD,CDKN2B-AS1,LINC00032,LINGO2,LINC01242,DDX58,PTPRD,BNC2,ANKRD18B
Controls
No Control Data Available
No Animal Model Data Available